# Hydroxyzine Hydrochloride

NDC: 68071-4499
Generic name: Hydroxyzine Hydrochloride
Labeler / Manufacturer: NuCare Pharmaceuticals,Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20130219

FDA application: ANDA088617

## Active ingredients

- HYDROXYZINE DIHYDROCHLORIDE: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68071-4499"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68071-4499
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=714a26a1-371f-ef23-e053-2a95a90a6af6